ENST00000269980.7:c.1001G>T
MANE Select
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ENSP00000269980.2:p.Gly334Val
|
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ENST00000269980.6:c.1001G>T
|
ENSP00000269980.2:p.Gly334Val
|
|
ENST00000457836.6:c.1010G>T
|
ENSP00000416000.2:p.Gly337Val
|
|
ENST00000540732.3:c.1103G>T
|
ENSP00000443246.1:p.Gly368Val
|
|
ENST00000542943.5:c.914G>T
|
ENSP00000440345.1:p.Gly305Val
|
|
ENST00000595085.5:c.922+306G>T
|
ENSP00000471150.2:n.922+306G>T
|
|
NM_000709.3:c.1001G>T
|
NP_000700.1:p.Gly334Val
|
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NM_001164783.1:c.998G>T
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NP_001158255.1:p.Gly333Val
|
|
NM_000709.4:c.1001G>T
MANE Select
|
NP_000700.1:p.Gly334Val
|
|
NM_001164783.2:c.998G>T
|
NP_001158255.1:p.Gly333Val
|
|